Variant DetailsVariant: esv3892663 Internal ID | 18836797 | Landmark | | Location Information | | Cytoband | 15q14 | Allele length | Assembly | Allele length | hg38 | 89276 | hg19 | 89276 | hg18 | 89276 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv25778429, essv25800887, essv25800762, essv25800489, essv25782274, essv25796268, essv25785175, essv25781059, essv25796055, essv25791023, essv25788222, essv25780529, essv25797986, essv25796632, essv25797530, essv25792505, essv25781704, essv25800527, essv25786156, essv25785920, essv25800210, essv25779032, essv25797581, essv25796564, essv25794866, essv25781274, essv25794974, essv25796675, essv25786687, essv25796650, essv25789403, essv25784446, essv25797301, essv25792961, essv25780382, essv25793343, essv25798698, essv25792618, essv25800943, essv25786194, essv25780090, essv25798443, essv25798050, essv25797913, essv25797595, essv25790997, essv25796525, essv25796294, essv25786179, essv25782975, essv25796652, essv25797147, essv25782636, essv25796410, essv25786562, essv25796111, essv25796442, essv25796080, essv25797903, essv25792659, essv25797783, essv25785393, essv25800472, essv25780818, essv25792648, essv25796153, essv25798854, essv25796769, essv25784753, essv25781558, essv25786890, essv25789365, essv25796941, essv25796176, essv25786383, essv25786429, essv25782664, essv25800163, essv25801402, essv25800068, essv25797909, essv25794459, essv25796116, essv25793425, essv25785103, essv25779118, essv25796707, essv25781016, essv25797043, essv25800694, essv25800533, essv25787681, essv25796192, essv25799380, essv25797625, essv25800922, essv25797629, essv25792810, essv25786238, essv25796032, essv25797376, essv25786361, essv25783833, essv25782347, essv25780509, essv25794782, essv25783739, essv25779231, essv25800575, essv25800347, essv25799913, essv25798062, essv25791577, essv25778505, essv25797098, essv25797024, essv25786038, essv25801241, essv25793158, essv25787881, essv25798055, essv25779621, essv25800405, essv25799956, essv25781638, essv25795333, essv25798075, essv25787427, essv25780229, essv25778293, essv25797417, essv25795015, essv25797398, essv25779950, essv25783300, essv25796541, essv25778444, essv25801021, essv25800267, essv25797138, essv25784679, essv25779632, essv25783418, essv25782405, essv25784344, essv25786042, essv25784721, essv25797708, essv25796425, essv25792678, essv25782457, essv25778414, essv25785317, essv25798238, essv25801500, essv25798315, essv25787937, essv25786182, essv25800552, essv25796431, essv25800831, essv25797090, essv25796236, essv25786574, essv25797129, essv25795994, essv25780343, essv25788769 | Samples | | Known Genes | GOLGA8A | Method | SNP array | Analysis | | Platform | Illumina HumanHap 550 Illumina HumanHap 610 Illumina Human OmniExpress | Comments | | Reference | Suktitipat_et_al_2014 | Pubmed ID | 25118596 | Accession Number(s) | esv3892663
| Frequency | Sample Size | 3017 | Observed Gain | 15 | Observed Loss | 153 | Observed Complex | 0 | Frequency | n/a |
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